196 related articles for article (PubMed ID: 28648510)
1. Disorders of H
Muzza M; Fugazzola L
Best Pract Res Clin Endocrinol Metab; 2017 Mar; 31(2):225-240. PubMed ID: 28648510
[TBL] [Abstract][Full Text] [Related]
2. DUOX Defects and Their Roles in Congenital Hypothyroidism.
De Deken X; Miot F
Methods Mol Biol; 2019; 1982():667-693. PubMed ID: 31172499
[TBL] [Abstract][Full Text] [Related]
3. Conformation of the N-Terminal Ectodomain Elicits Different Effects on DUOX Function: A Potential Impact on Congenital Hypothyroidism Caused by a H
Louzada RA; Corre R; Ameziane-El-Hassani R; Hecht F; Cazarin J; Buffet C; Carvalho DP; Dupuy C
Thyroid; 2018 Aug; 28(8):1052-1062. PubMed ID: 29845893
[TBL] [Abstract][Full Text] [Related]
4. The Dual Oxidase Duox2 stabilized with DuoxA2 in an enzymatic complex at the surface of the cell produces extracellular H
Poncelet L; Dumont JE; Miot F; De Deken X
Exp Cell Res; 2019 Nov; 384(1):111620. PubMed ID: 31513783
[TBL] [Abstract][Full Text] [Related]
5. Genetic defects of hydrogen peroxide generation in the thyroid gland.
Weber G; Rabbiosi S; Zamproni I; Fugazzola L
J Endocrinol Invest; 2013 Apr; 36(4):261-6. PubMed ID: 23404134
[TBL] [Abstract][Full Text] [Related]
6. DUOXS defects: Genotype-phenotype correlations.
Fugazzola L; Muzza M; Weber G; Beck-Peccoz P; Persani L
Ann Endocrinol (Paris); 2011 Apr; 72(2):82-6. PubMed ID: 21511237
[TBL] [Abstract][Full Text] [Related]
7. Inhibition of the thyroid hormonogenic H
Giusti N; Gillotay P; Trubiroha A; Opitz R; Dumont JE; Costagliola S; De Deken X
Mol Cell Endocrinol; 2020 Jan; 500():110635. PubMed ID: 31678421
[TBL] [Abstract][Full Text] [Related]
8. [Genetic analysis of TPO, DUOX2 and DUOXA2 genes in children with permanent congenital hypothyroidism suspected dyshormonogenesis].
Huang YL; Tan MY; Jiang X; Li B; Chen QY; Jia XF; Tang CF; Liu JL; Liu L
Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):210-214. PubMed ID: 28273705
[No Abstract] [Full Text] [Related]
9. New phenotypes in thyroid dyshormonogenesis: hypothyroidism due to DUOX2 mutations.
Moreno JC; Visser TJ
Endocr Dev; 2007; 10():99-117. PubMed ID: 17684392
[TBL] [Abstract][Full Text] [Related]
10.
Wang F; Zang Y; Li M; Liu W; Wang Y; Yu X; Li H; Wang F; Liu S
Front Endocrinol (Lausanne); 2020; 11():237. PubMed ID: 32425884
[No Abstract] [Full Text] [Related]
11.
Peters C; Nicholas AK; Schoenmakers E; Lyons G; Langham S; Serra EG; Sebire NJ; Muzza M; Fugazzola L; Schoenmakers N
Thyroid; 2019 Jun; 29(6):790-801. PubMed ID: 31044655
[No Abstract] [Full Text] [Related]
12. A novel missense mutation (I26M) in DUOXA2 causing congenital goiter hypothyroidism impairs NADPH oxidase activity but not protein expression.
Liu S; Liu L; Niu X; Lu D; Xia H; Yan S
J Clin Endocrinol Metab; 2015 Apr; 100(4):1225-9. PubMed ID: 25675383
[TBL] [Abstract][Full Text] [Related]
13. Functional Characterization of DUOX Enzymes in Reconstituted Cell Models.
Korzeniowska A; Donkó ÁP; Morand S; Leto TL
Methods Mol Biol; 2019; 1982():173-190. PubMed ID: 31172473
[TBL] [Abstract][Full Text] [Related]
14. Genetic Evaluation of Congenital Hypothyroidism with Gland
Shin JH; Kim HY; Kim YM; Lee H; Bae MH; Park KH; Lee SM; Kwak MJ
Ann Clin Lab Sci; 2021 Jan; 51(1):73-81. PubMed ID: 33653783
[TBL] [Abstract][Full Text] [Related]
15. Mice deficient in dual oxidase maturation factors are severely hypothyroid.
Grasberger H; De Deken X; Mayo OB; Raad H; Weiss M; Liao XH; Refetoff S
Mol Endocrinol; 2012 Mar; 26(3):481-92. PubMed ID: 22301785
[TBL] [Abstract][Full Text] [Related]
16. Compound heterozygosity for a novel hemizygous missense mutation and a partial deletion affecting the catalytic core of the H2O2-generating enzyme DUOX2 associated with transient congenital hypothyroidism.
Hoste C; Rigutto S; Van Vliet G; Miot F; De Deken X
Hum Mutat; 2010 Apr; 31(4):E1304-19. PubMed ID: 20187165
[TBL] [Abstract][Full Text] [Related]
17. Genetic causes of congenital hypothyroidism due to dyshormonogenesis.
Grasberger H; Refetoff S
Curr Opin Pediatr; 2011 Aug; 23(4):421-8. PubMed ID: 21543982
[TBL] [Abstract][Full Text] [Related]
18. A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion.
Hulur I; Hermanns P; Nestoris C; Heger S; Refetoff S; Pohlenz J; Grasberger H
J Clin Endocrinol Metab; 2011 May; 96(5):E841-5. PubMed ID: 21367925
[TBL] [Abstract][Full Text] [Related]
19. Hypothyroidism-associated missense mutation impairs NADPH oxidase activity and intracellular trafficking of Duox2.
Donkó Á; Morand S; Korzeniowska A; Boudreau HE; Zana M; Hunyady L; Geiszt M; Leto TL
Free Radic Biol Med; 2014 Aug; 73():190-200. PubMed ID: 24853759
[TBL] [Abstract][Full Text] [Related]
20. Compound Heterozygous Mutations in the DUOX2/DUOXA2 Genes Cause Congenital Hypothyroidism.
Zheng X; Ma SG; Guo ML; Qiu YL; Yang LX
Yonsei Med J; 2017 Jul; 58(4):888-890. PubMed ID: 28541007
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
